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SYNCHRON EL-ISE(TM) ELECTROLYTE SYSTEMS

K897183 Class II Traditional
Decision Date
1990-03-30
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K897183
Product Code JFL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 1990-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON EL-ISE(TM) ELECTROLYTE SYSTEMS received FDA 510(k) clearance under submission number K897183, sponsored by Beckman Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1990-03-30.

Classification & Regulation

This clearance is catalogued under FDA product code JFL and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.